Excitation Of Coherent Phonons Research Articles

Killer Phonon Caught: Femtosecond Stimulated Raman Spectroscopy Identifies Phonon-Induced Control of Photophysics in Rubrene Derivatives.

Molecular reaction coordinates are defined by the interplay of a number of orthogonal nuclear coordinates and are inherently multidimensional for large molecules. Identifying how specific nuclear motions along these reaction coordinates can be used to drive and control chemical processes is a promising approach for the optimization of chemical outcomes and targeted synthetic design. Here, we used femtosecond stimulated Raman spectroscopy (FSRS) to quantify the effects of individual phonon nuclear motions on singlet fission in rubrene derivatives. Rubrene readily undergoes singlet fission and is amendable to chemical derivatization, yet the factors that impact the singlet fission yield are not fully understood. Crystal packing is known to play a significant role in both fission and carrier transport, and thus, we focused on the impact of phonon nuclear motions on the photophysics. We used four halogen-substituted rubrene crystals and successfully identified one specific phonon mode that suppresses singlet fission in these crystals. We used FSRS with single-pulse excitation and double-pulse excitation to coherently amplify each phonon mode and quantify its effects on the excited-state process. We found that coherent amplification of the specific phonon vibration involving twisting of the peripheral phenyl rings and tetracene core motions resulted in less ground-state depletion and fewer triplet state absorption. Our study demonstrated that it is possible to use coherent phonon excitation to influence the photophysical outcome, while also showing that FSRS with double-pulse excitation can be a successful tool for quantifying mode-selective contributions to photophysics.

Unzipping hBN with ultrashort mid-infrared pulses.

Manipulating the nanostructure of materials is critical for numerous applications in electronics, magnetics, and photonics. However, conventional methods such as lithography and laser writing require cleanroom facilities or leave residue. We describe an approach to creating atomically sharp line defects in hexagonal boron nitride (hBN) at room temperature by direct optical phonon excitation with a mid-infrared pulsed laser from free space. We term this phenomenon "unzipping" to describe the rapid formation and growth of a crack tens of nanometers wide from a point within the laser-driven region. Formation of these features is attributed to the large atomic displacement and high local bond strain produced by strongly driving the crystal at a natural resonance. This process occurs only via coherent phonon excitation and is highly sensitive to the relative orientation of the crystal axes and the laser polarization. Its cleanliness, directionality, and sharpness enable applications such as polariton cavities, phonon-wave coupling, and in situ flake cleaving.

Terahertz sum-frequency excitation of coherent optical phonons in the two-dimensional semiconductor WSe2

Driving fundamental excitations via strong light fields is one of the most important issues in solid state physics, which opens up new avenues to control material properties. Two-dimensional materials are fruitful platforms for future semiconductor applications, including opto-electronic and phononic devices, yet the phonon dynamics and nonlinear phonon–phonon coupling remain under-explored. Here, we demonstrate coherent phonon excitation in thin films of the layered two-dimensional semiconductor WSe2 induced by intense and broadband ultrafast terahertz (THz) pulses. We performed THz Kerr effect spectroscopy and observed coherent phonon oscillations assigned to the E2g optical phonon mode. The phonon amplitude displays a quadratic THz field strength dependence, indicating a sum-frequency THz excitation process. Furthermore, pump–probe polarization and crystal orientation relationships, supported by symmetry analysis of the nonlinear susceptibility and Raman tensors, provide helpful insight into nonlinear phonon–phonon interactions and potential coherent control schemes for the manipulation of phonon polarization and material properties in WSe2.

Precision-controlled ultrafast electron microscope platforms. A case study: Multiple-order coherent phonon dynamics in 1T-TaSe2 probed at 50 fs-10 fm scales.

We report on the first detailed beam tests attesting the fundamental principle behind the development of high-current-efficiency ultrafast electron microscope systems where a radio frequency (RF) cavity is incorporated as a condenser lens in the beam delivery system. To allow for the experiment to be carried out with a sufficient resolution to probe the performance at the emittance floor, a new cascade loop RF controller system is developed to reduce the RF noise floor. Temporal resolution at 50 fs in full-width-at-half-maximum and detection sensitivity better than 1% are demonstrated on exfoliated 1T-TaSe2 system under a moderate repetition rate. To benchmark the performance, multi-terahertz edge-mode coherent phonon excitation is employed as the standard candle. The high temporal resolution and the significant visibility to very low dynamical contrast in diffraction signals via high-precision phase-space manipulation give strong support to the working principle for the new high-brightness femtosecond electron microscope systems.

Coherent Phonon Manipulation via Electron-Phonon Interaction for Facilitated Relaxation of Metastable Centers in ZnO.

Methods that allow versatile manipulation of metastable centers in semiconductors are highly important owing to their potential for quantum information processing and computations. In this study, we demonstrate that the electron-phonon interaction enables phonon participation to promote relaxation of metastable centers in ZnO, which is known for its persistent photoconductivity (PPC) effect. Experimentally, we show that continuous infrared (IR) radiation (1064 nm, ∼30 mW/cm2) promotes longitudinal optical phonons via the Fröhlich interaction and increases the PPC relaxation rate by ∼4 folds. More importantly, we discover that coherent phonons activated by an ultrashort pulse IR laser of the same power increased the relaxation rate by ∼1200-fold, as confirmed by ultrafast transient spectroscopy to be correlated to the excitation of coherent acoustic phonons via the inverse piezoelectric effect. We expect this study to provide valuable guidance for the development of novel quantum and photoactive devices.

Giant acceleration of polaron transport by ultrafast laser-induced coherent phonons.

Polaron formation is ubiquitous in polarized materials, but severely hampers carrier transport for which effective controlling methods are urgently needed. Here, we show that laser-controlled coherent phonon excitation enables orders of magnitude enhancement of carrier mobility via accelerating polaron transport in a prototypical material, lithium peroxide (Li2O2). The selective excitation of specific phonon modes, whose vibrational pattern directly overlap with the polaronic lattice deformation, can remarkably reduce the energy barrier for polaron hopping. The strong nonadiabatic couplings between the electronic and ionic subsystem play a key role in triggering the migration of polaron, via promoting phonon-phonon scattering in q space within sub-picoseconds. These results extend our understanding of polaron transport dynamics to the nonequilibrium regime and allow for optoelectronic devices with ultrahigh on-off ratio and ultrafast responsibility, competitive with those of state-of-the-art devices fabricated based on free electron transport.

Dispersion of optical constants of Si:PbGeO crystal in the terahertz range

Objectives. Advances in laser physics over the last decade have led to the creation of sources of single-period electromagnetic pulses having a duration of about 1 ps, corresponding to the terahertz (THz) frequency range and a field amplitude of several tens of MV/cm. This allows the electrode-free application of an electric field to a ferroelectric for observing not only the excitation of coherent phonons, but also ultrafast (at the sub-picosecond timescale) dynamic polarization switching. To detect polarization switching, a pump-probe technique is used in which a THz pulse is used with an optical probe. Since its intensity is proportional to the square of the polarization, the signal of the optical second harmonic is used to measure polarization switching under the action of a THz pulse. To evaluate switching efficiency, both linear (refractive index and absorption coefficient) and non-linear optical characteristics (quadratic and cubic susceptibilities) are required. For any application of ferroelectric crystals in the THz range, knowledge of the relevant linear optical characteristics is also necessary.Methods. The technique of THz spectroscopy in the time domain was used; here, a picosecond THz pulse transmitted through the crystal is recorded by strobing the detector with a femtosecond optical pulse. The THz-induced dynamics of the order parameter in a ferroelectric was studied by detecting the intensity of a nonlinear optical signal at the frequency of the second optical harmonic.Results. The transmission of a THz wave and the intensity of second harmonic generation on a lead germanate crystal doped with silicon in the time and spectral domains were measured. On this basis, the absorption coefficient dispersion and cubic nonlinear susceptibility were calculated in the range of 0.5-2.0 THz. The presence of a region of fundamental absorption near the phonon modes was confirmed along with a resonant enhancement of the cubic nonlinear susceptibility for two phonon modes Ω1 = 1.3 THz and Ω2 = 2.0 THz.Conclusions. The proposed technique is effective for analyzing the dispersion of the optical characteristics of ferroelectric crystals. The significantly improved spectral resolution (0.1 THz) increases the accuracy of determining nonlinear susceptibility due to the detailed analysis of the linear and nonlinear contributions to the second harmonic intensity.

Quantum pathways of carrier and coherent phonon excitation in bismuth

Ultrafast mid-infrared excitation of an electron-hole plasma breaks the crystal symmetry of bismuth transiently and opens alternative quantum pathways for the excitation of coherent lattice motions. Probing the transient crystal structure directly by femtosecond x-ray diffraction reveals oscillations of diffracted intensity at a frequency of 2.6 THz, which persist on a picosecond time scale. They reflect coherent wave packet motions along back-folded phonon coordinates in the crystal of reduced symmetry. Optically induced symmetry breaking thus allows for modifying phonon excitations.

Towards chiral acoustoplasmonics.

The possibility of creating and manipulating nanostructured materials encouraged the exploration of new strategies to control electromagnetic properties. Among the most intriguing nanostructures are those that respond differently to helical polarization, i.e., exhibit chirality. Here, we present a simple structure based on crossed elongated bars where light-handedness defines the dominating cross-section absorption or scattering, with a 200 % difference from its counterpart (scattering or absorption). The proposed chiral system opens the way to enhanced coherent phonon excitation and detection. We theoretically propose a simple coherent phonon generation (time-resolved Brillouin scattering) experiment using circularly polarized light. In the reported structures, the generation of acoustic phonons is optimized by maximizing the absorption, while the detection is enhanced at the same wavelength and different helicity by engineering the scattering properties. The presented results constitute one of the first steps towards harvesting chirality effects in the design and optimization of efficient and versatile acoustoplasmonic transducers.

Quantum theory of light-driven coherent lattice dynamics

The exposure to intense electromagnetic radiation can induce distortions and symmetry breaking in the crystal structure of solids, providing a route for the all-optical control of their properties. In this manuscript, we formulate a unified theoretical approach to describe the coherent lattice dynamics in presence of external driving fields, electron-phonon and phonon-phonon interactions, and quantum nuclear effects. The main mechanisms for the excitation of coherent phonons - including infrared absorption, displacive excitation, inelastic stimulated Raman scattering, and ionic Raman scattering - can be seamlessly accounted for. We apply this formalism to a model consisting of two coupled phonon modes, where we illustrate the influence of quantum nuclei on structural distortions induced by ionic Raman scattering. Besides validating the widely-employed classical models for the coherent lattice dynamics, our work provides a versatile approach to methodically explore the emergence of quantum nuclear effects in the structural response of crystal lattice to strong fields.

Resonance-enhanced excitation and relaxation dynamics of coherent phonons in Fe1.14Te.

Lattice dynamics plays a significant role in manipulating the unique physical properties of materials. In this work, femtosecond transient optical spectroscopy is used to investigate the generation mechanism and relaxation dynamics of coherent phonons in Fe1.14Te-a parent compound of chalcogenide superconductors. The reflectivity time series consist of the exponential decay component due to hot carriers and damped oscillations caused by the A1g phonon vibration. The vibrational frequency and dephasing time of the A1g phonons are obtained as a function of temperature. With increasing temperature, the phonon frequency decreases and can be well described with the anharmonicity model. Dephasing time is independent of temperature, indicating that the phonon dephasing is dominated by phonon-defect scattering. The impulsive stimulated Raman scattering mechanism is responsible for the coherent phonon generation. Owing to the resonance Raman effect, the maximum photosusceptibility of the A1g phonons occurs at 1.590 eV, corresponding to an electronic transition in Fe1.14Te.

Selective Excitation of Higher Harmonic Coherent Acoustic Phonons in a Graphite Nanofilm

Selective Excitation of Higher Harmonic Coherent Acoustic Phonons in a Graphite Nanofilm

Anti-Jahn-Teller effect induced ultrafast insulator to metal transition in perovskite BaBiO3

The Jahn-Teller (JT) effect involves the ions M with a degenerate electronic state distorting the corner-sharing MO6 octahedra to lift the degeneracy, inducing strong coupling of electrons to lattice, and mediating the exotic properties in perovskite oxides. Conversely, the anti-Jahn–Teller (AJT) effect refers to the deformation against the Jahn-Teller-distorted MO6 octahedra. However, it is difficult to experimentally execute both effects descending from the fine-tuning of crystal structures. We propose the AJT can be introduced by THz laser illumination at 11.71 THz in a candidate superconducting perovskite material BaBiO3 near room temperature. The illumination coherently drives the infrared-active phonon that excites the Raman breathing mode through the quadratic-linear nonlinear interaction. The process is characterized by the emergence of an AJT effect, accompanied by an insulator-to-metal transition occurring on the picosecond timescale. This study underlines the important role of crystal structure engineering by coherent phonon excitation in designing optoelectronic devices.

High-harmonic spectroscopy of coherent lattice dynamics in graphene

High-harmonic spectroscopy of solids is a powerful tool, which provides access to both electronic structure and ultrafast electronic response of solids, from their band structure and density of states to phase transitions, including the emergence of the topological edge states, to the PetaHertz electronic response. However, in spite of these successes, high-harmonic spectroscopy has hardly been applied to analyze the role of coherent femtosecond lattice vibrations in the attosecond electronic response. Here we study coherent phonon excitations in monolayer graphene to show how high-harmonic spectroscopy can be used to detect the influence of coherent lattice dynamics, particularly longitudinal and transverse optical phonon modes, on the electronic response. Coherent excitation of the in-plane phonon modes results in the appearance of sidebands in the spectrum of the emitted harmonic radiation. We show that the spectral positions and the polarization of the sideband emission offer a sensitive probe of the dynamical symmetries associated with the excited phonon modes. Our work brings the key advantage of high-harmonic spectroscopy---the combination of subfemtosecond to tens of femtoseconds temporal resolution---to the problem of probing phonon-driven electronic response and its dependence on the dynamical symmetries in solids.

Spectrally Resolving the Phase and Amplitude of Coherent Phonons in the Charge Density Wave State of 1T‐TaSe2

AbstractThe excitation and detection of coherent phonons have given unique insights into the condensed matter, in particular for materials with strong electron–phonon coupling. A study of coherent phonons is reported in the layered charge density wave (CDW) compound 1T‐TaSe2 performed using transient broadband reflectivity spectroscopy, in the photon energy range 1.75–2.65 eV. Several intense and long‐lasting (>20 ps) oscillations, arising from the CDW superlattice reconstruction, are observed allowing for detailed analysis of the spectral dependence of their amplitude and phase. For energies above 2.4 eV, where transitions involve Ta d‐bands, the CDW amplitude mode at 2.19 THz is found to dominate the coherent response. At lower energies, instead, beating arises between additional frequencies, with a particularly intense mode at 2.95 THz. Interestingly, the spectral analysis reveals a π phase shift at 2.4 eV. Results are discussed considering the selective coupling of specific modes to energy bands involved in the optical transitions seen in steady‐state reflectivity. The work demonstrates how coherent phonon spectroscopy can distinguish and resolve optical states strongly coupled to the CDW order and provide additional information normally hidden in conventional steady‐state techniques.

Anisotropic electron and lattice dynamics in excitonic insulator Ta2NiSe5

We employ polarization-resolved femtosecond optical pump–probe spectroscopy to investigate the nonequilibrium photocarrier dynamics in excitonic insulator Ta2NiSe5. The electronic dynamics, including hot carrier cooling, exciton formation, and recombination in the timescale ranging from subpicoseconds to a few tens of picoseconds, have been established from the transient reflectivity spectra, showing strong in-plane anisotropy with respect to the probe polarization. Such anisotropic photocarrier dynamics possibly arise from the crystalline orientation dependence of the excitonic polarizability. Furthermore, we find that the amplitude of coherent phonons with a frequency of 1 THz is subject to the probe polarization, whereas it is not sensitive to the pump polarization. This substantiates that the displacive excitation of coherent phonons plays a decisive role in lattice dynamics. In addition, we find that the photo-induced dielectric screening tends to suppress the amplitude of coherent phonons with increasing pump fluence, manifesting a remarkable polarization dependence. Our work provides valuable insights into the excitonic dynamics and the origin of coherent phonon generation and also may contribute to the development of polarization-sensitive photoelectric devices based on Ta2NiSe5.

Terahertz displacive excitation of a coherent Raman-active phonon in V2O3

Nonlinear processes involving frequency-mixing of light fields set the basis for ultrafast coherent spectroscopy of collective modes in solids. In certain semimetals and semiconductors, generation of coherent phonon modes can occur by a displacive force on the lattice at the difference-frequency mixing of a laser pulse excitation on the electronic system. Here, as a low-frequency counterpart of this process, we demonstrate that coherent phonon excitations can be induced by the sum-frequency components of an intense terahertz light field, coupled to intraband electronic transitions. This nonlinear process leads to charge-coupled coherent dynamics of Raman-active phonon modes in the strongly correlated metal V2O3. Our results show an alternative up-conversion pathway for the optical control of Raman-active modes in solids mediated by terahertz-driven electronic excitation.

Intracavity Raman scattering couples soliton molecules with terahertz phonons

Ultrafast atomic vibrations mediate heat transport, serve as fingerprints for chemical bonds and drive phase transitions in condensed matter systems. Light pulses shorter than the atomic oscillation period can not only probe, but even stimulate and control collective excitations. In general, such interactions are performed with free-propagating pulses. Here, we demonstrate intra-cavity excitation and time-domain sampling of coherent optical phonons inside an active laser oscillator. Employing real-time spectral interferometry, we reveal that Terahertz beats of Raman-active optical phonons are the origin of soliton bound-states – also termed “Soliton molecules” – and we resolve a coherent coupling mechanism of phonon and intra-cavity soliton motion. Concurring electronic and nuclear refractive nonlinearities generate distinct soliton trajectories and, effectively, enhance the time-domain Raman signal. We utilize the intrinsic soliton motion to automatically perform highspeed Raman spectroscopy of the intra-cavity crystal. Our results pinpoint the impact of Raman-induced soliton interactions in crystalline laser media and microresonators, and offer unique perspectives toward ultrafast nonlinear phononics by exploiting the coupling of atomic motion and solitons inside a cavity.

Interlayer magnetophononic coupling in MnBi2Te4

The emergence of magnetism in quantum materials creates a platform to realize spin-based applications in spintronics, magnetic memory, and quantum information science. A key to unlocking new functionalities in these materials is the discovery of tunable coupling between spins and other microscopic degrees of freedom. We present evidence for interlayer magnetophononic coupling in the layered magnetic topological insulator MnBi2Te4. Employing magneto-Raman spectroscopy, we observe anomalies in phonon scattering intensities across magnetic field-driven phase transitions, despite the absence of discernible static structural changes. This behavior is a consequence of a magnetophononic wave-mixing process that allows for the excitation of zone-boundary phonons that are otherwise ‘forbidden’ by momentum conservation. Our microscopic model based on density functional theory calculations reveals that this phenomenon can be attributed to phonons modulating the interlayer exchange coupling. Moreover, signatures of magnetophononic coupling are also observed in the time domain through the ultrafast excitation and detection of coherent phonons across magnetic transitions. In light of the intimate connection between magnetism and topology in MnBi2Te4, the magnetophononic coupling represents an important step towards coherent on-demand manipulation of magnetic topological phases.

Phonon-Induced Relocation of Valence Charge in Boron Nitride Observed by Ultrafast X-Ray Diffraction.

The impact of coherent phonon excitations on the valence charge distribution in cubic boron nitride is mapped by femtosecond x-ray powder diffraction. Zone-edge transverse acoustic (TA) two-phonon excitations generated by an impulsive Raman process induce a steplike increase of diffracted x-ray intensity. Charge density maps derived from transient diffraction patterns reveal a spatial transfer of valence charge from the interstitial region onto boron and nitrogen atoms. This transfer is modulated with a frequency of 250GHz due to a coherent superposition of TA phonons related to the ^{10}B and ^{11}B isotopes. Nuclear and electronic degrees of freedom couple through many-body Coulomb interactions.